AU622303B2 - Method of optimizing texture and processability of chewing gums and compositions made therefrom - Google Patents
Method of optimizing texture and processability of chewing gums and compositions made therefrom Download PDFInfo
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- AU622303B2 AU622303B2 AU52300/90A AU5230090A AU622303B2 AU 622303 B2 AU622303 B2 AU 622303B2 AU 52300/90 A AU52300/90 A AU 52300/90A AU 5230090 A AU5230090 A AU 5230090A AU 622303 B2 AU622303 B2 AU 622303B2
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- Prior art keywords
- sorbitol
- gum
- gums
- powders
- powdered
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- 239000000203 mixture Substances 0.000 title claims description 72
- 238000000034 method Methods 0.000 title claims description 37
- 235000015218 chewing gum Nutrition 0.000 title claims description 24
- 235000010356 sorbitol Nutrition 0.000 claims description 159
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 157
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 154
- 239000000600 sorbitol Substances 0.000 claims description 154
- 239000000843 powder Substances 0.000 claims description 49
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 42
- 238000009472 formulation Methods 0.000 claims description 37
- 239000000796 flavoring agent Substances 0.000 claims description 36
- 235000019634 flavors Nutrition 0.000 claims description 36
- 230000008569 process Effects 0.000 claims description 22
- 235000011187 glycerol Nutrition 0.000 claims description 21
- 229940112822 chewing gum Drugs 0.000 claims description 20
- 239000004615 ingredient Substances 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 239000004014 plasticizer Substances 0.000 claims description 12
- 101000801619 Homo sapiens Long-chain-fatty-acid-CoA ligase ACSBG1 Proteins 0.000 claims description 11
- 102100033564 Long-chain-fatty-acid-CoA ligase ACSBG1 Human genes 0.000 claims description 11
- 235000010634 bubble gum Nutrition 0.000 claims description 11
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 239000000945 filler Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 7
- 239000004067 bulking agent Substances 0.000 claims description 6
- 239000003086 colorant Substances 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 6
- 235000003599 food sweetener Nutrition 0.000 claims description 5
- 239000003765 sweetening agent Substances 0.000 claims description 5
- 229920001908 Hydrogenated starch hydrolysate Polymers 0.000 claims description 4
- 235000007983 food acid Nutrition 0.000 claims description 4
- 238000012545 processing Methods 0.000 claims description 4
- 235000020357 syrup Nutrition 0.000 claims description 3
- 239000006188 syrup Substances 0.000 claims description 3
- 235000009754 Vitis X bourquina Nutrition 0.000 claims description 2
- 235000012333 Vitis X labruscana Nutrition 0.000 claims description 2
- 240000006365 Vitis vinifera Species 0.000 claims description 2
- 235000014787 Vitis vinifera Nutrition 0.000 claims description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 claims 5
- 239000008123 high-intensity sweetener Substances 0.000 claims 2
- 235000013615 non-nutritive sweetener Nutrition 0.000 claims 2
- 239000002245 particle Substances 0.000 description 42
- 238000009826 distribution Methods 0.000 description 17
- 230000000717 retained effect Effects 0.000 description 12
- HIMQVZDNGULBFJ-HUNMEVQMSA-N (2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO HIMQVZDNGULBFJ-HUNMEVQMSA-N 0.000 description 10
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- 238000012360 testing method Methods 0.000 description 7
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 6
- 229930195725 Mannitol Natural products 0.000 description 6
- 239000000594 mannitol Substances 0.000 description 6
- 235000010355 mannitol Nutrition 0.000 description 6
- 108010011485 Aspartame Proteins 0.000 description 5
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 5
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 4
- 235000014755 Eruca sativa Nutrition 0.000 description 4
- 244000024675 Eruca sativa Species 0.000 description 4
- 239000000605 aspartame Substances 0.000 description 4
- 235000010357 aspartame Nutrition 0.000 description 4
- 229960003438 aspartame Drugs 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 230000001788 irregular Effects 0.000 description 4
- 235000010445 lecithin Nutrition 0.000 description 4
- 239000000787 lecithin Substances 0.000 description 4
- 229940067606 lecithin Drugs 0.000 description 4
- 238000007873 sieving Methods 0.000 description 4
- 238000005457 optimization Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 240000004181 Eucalyptus cladocalyx Species 0.000 description 1
- 235000016623 Fragaria vesca Nutrition 0.000 description 1
- 240000009088 Fragaria x ananassa Species 0.000 description 1
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 1
- 235000014749 Mentha crispa Nutrition 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 244000078639 Mentha spicata Species 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Natural products C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 description 1
- UOAITRWPAYGGAM-UHFFFAOYSA-L calcium;propane-1,2,3-triol;carbonate Chemical compound [Ca+2].[O-]C([O-])=O.OCC(O)CO UOAITRWPAYGGAM-UHFFFAOYSA-L 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000010961 commercial manufacture process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000008369 fruit flavor Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000008447 perception Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
- A23G4/10—Chewing gum characterised by the composition containing organic or inorganic compounds characterised by the carbohydrates used, e.g. polysaccharides
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/18—Chewing gum characterised by shape, structure or physical form, e.g. aerated products
- A23G4/20—Composite products, e.g. centre-filled, multi-layer, laminated
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S426/00—Food or edible material: processes, compositions, and products
- Y10S426/804—Low calorie, low sodium or hypoallergic
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Confectionery (AREA)
- Seasonings (AREA)
Description
i i i .aLI- 622303 S F Ref: 77010D1 FORM COMMONWEALTH OF AUSTRALIA PATENTS ACT 1952 COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE: Class Int Class 0@ Complete Specification Lodged: Accepted.
Published: Priority: Related Art: Name and Address of Applicant: Wm. Wrigley Jr. Company 410 North Michigan Avenue Chicago Illinois 60611 UNITED STATES OF AMERICA Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Address for Service:
S
Complete Specification for the invention entitled: Method of Optimizing Texture and Prccessability of Chewing Gums and Compositions Made Therefrom The following statement is a full description of this invention, including the best method of performing it known to me/us 5845/6 _.1 j
I
i Ya pi ii wi -1 s~~ ABSTRACT OF THE DISCLOSURE A method of optimizing texture and processability of chewing gum compositions is disclosed. The method includes the steps of making a sample batch of chewing gum containing powdered sorbitol, making subsequent batches of gum also using powdered sorbitol, using at least two types of powdered sorbitol in one or more of the samples batches and varying the ratio between the at least two types of powdered sorbitol between sample batches in order to optimize texture and processability of the gum. The types of powdered sorbitol may differ in their particle size distribution or particle morphology. Also, the differences in types of powdered sorbitol may be evaluated by making a standard sorbitol property testing (SSPT) gum formula and measuring the Taber and Instron hardness of standard stickes of the resulting gum. Methods of manufacturing gum vind gm ompositions using optimized ratios of powdered sorbitul are also disclosed.
I METHOD OF OPTIMIZING TEXTURE AND PROCESSABILITY OF CHEWING GUMS AND COMPOSITIONS MADE THEREFROM BACKGROUND OF THE INVENTION The present invention relates to chewing gum compositions and manufacturing methods. In particular, the invention relates to methods of optimizing gum formulations for texture and processability characteristics, and, once optimized, producing gum compositions with the optimized formulation.
cei One difficulty encountered in reformulating Schewing gum compositions to implement various desired ingredient changes, or in developing new formulations, is that the final texture of the new compositions and the processability characteristics associated with their manufacture cannot be determined without actually making sample batches of the gum. This is due to the fact that gum compositions are quite complex systems, containing a gum base (which in itself is usually made from several ingredients), bulking and sweetening *h~r 2 agents, plasticizers, fillers, flavors, colors and numerous other ingredients.
Thus, when one ingredient is changed, even one present in small amounts such as the flavor, it is often necessary to make up repeated sample batches of gum using the new ingredient, adjusting the levels of other ingredients in each batch until a gum formulation is reached which has the desired properties. Not only must the final gum texture and other properties be acceptable, but the processability characteristics of the gum should be such that the gum can be made using existing machinery and production techniques.
A major reformulation is very costly and time consuming. To reduce costs, new formulations are generally made up on a small scale while working out an 0 acceptable formulation, and then the formulation is further refined on production scale equipment until its processability is acceptable.
.The aforementioned problems are particularly 0 acute in the case of formulating a sugarless gum which is to be processed using the same equipment used to manufacture and wrap a sugar-gum.
For example, a sugar chunk gum is usually processed by passing the formulated gum through an extruder which formnis a rope. The extrusion requires the gum to be very pliable, which is accomplished by heating the gum before or during the extrusion to 1200 140 0 F. Before the gum can be cut into chunks and Swrapped, it is generally stretched and sized to reduce the extruded rope diameter, and must be cooled. The cooling and sizing is typically done in a cooling tunnel. To save space, the path through the tunnel is circuitous or serpentine in nature. In order to follow this path without breaking, the gum rope must still be flexible when it cools.
-2
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000 0
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0060 0
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CC
C C C S To account for variation in production rates between the extruder and the wrapping equipment, conventional chunk gum processing uses a "snaking table" after the cooling tunnel. The snaking table acts as a buffer, filling with gum rope when the wrapping speed is less than the extrusion speed, the excess being depleted when wrapping speeds are increased. It is imperative that the gum rope remain cohesive on the snaking table. Any break in the rope will require manual intervention to splice the rope or refeed it into the cutting and wrapping equipment.
The softness and flexibility required in the cooling tunnel and on the snaking table must be coupled with firmness if the gum is to be successfully cut and wrapped. If the gum is too soft or sticky, it will be smeared by the cutting equipment and be impossible to wrap. It is believed that because their gums do not have proper processability characteristics, some manufacturers of sugarless chunk gum cut the extruded rope into lengths and allow it to cool and set to the proper cutting and wrapping consistency. This procedure requires splicing the lengthsbefore feeding the rope into the cutting equipment, a time consuming and expensive procedure.
Besides the difficulties in formulating sugarless gums for manufacturing processability, the formulations must also have proper softness and non-sticky texture characteristics in its finished state, with proper sweetness and flavor release attributes, to be acceptable to a majority of consumers. Optimizing both this final texture and the processability at the same time has been a time consuming and expensive task.
3 ~is I'iIg; ~i 4 l SUMMARY OF THE INVENTION Accordingly, a method of optimizing texture and processability of chewing gums containing sorbitol is provided according to the present invention wherein at least two types of powdered sorbitol are used in making sample batches of the gum, and the ratio between the two types of powdered sorbitol is varied between sample batches in order to optimize texture and processability of the gum. The differences between the at least two types of powdered sorbitol may be in their particle size distribution, or their particle morphology, as described more fully herein. The present application further discusses additional, but inherent properties of the powdered sorbitol which can be measured by using standard equipment and S procedures to measure the properties of gums made with the powdered sorbitol.
Once the formulation has been optimized, the invention also includes manufacturing the gum by using the at least two types of powdered sorbitol at the optimized ratio. The invention also includes gums manufactured by this process.
.By using at least two types of powdered sorbitol in formulating gum composition, it is possible to quickly optimize the formulation while varying only one parameter, the ratio between the types of sorbitol.
It has been found that by using just two types of sorbitol, a sugarless gum formulation can be altered S(such as by changing the flavor) and the new formulation can be quickly optimized with respect to texture and processability without changing any ingredient levels other than the ratio of the two types of sorbitol powder.
4 j 4
S
S
S
S
0O *5
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*5*S S. C 5 BRIEF DESCRIPTION OF THE FIGURES Fig. 1 is a photograph of an enlarged view of powdered sorbitol particles having an ICI morphology.
Fig. 2 is a photograph of an enlarged view of powdered sorbitol particles having a Pfizer morphology.
DETAILED DESCRIPTION OF THE FIGURES AND OF THE PREFERRED EMBODIMENTS OF THE INVENTION The term chewing gum as used herein includes chewing gum, bubble gum and the like.
Chewing gum formulations comprise a matrix of a gum base, usually natural or synthetic blends, in a range of 20-35 percent by weight and typically percent; plasticizers in a range of 5-25 percent and typically 10 percent; glycerine in a range of 0-3 percent and typically 0-5 percent; bulking and/or sweetening agents in a range of 20-90 percent and typically 40 percent; and flavor in the range of 0.5-2 percent and typically 1 percent. High glycerine content gum may include 15-45 percent gum base, 25-60 percent powdeied sorbitol and 15-25 percent glycerine.
During development of this invention, applicants have been limited to using commercially available types of powdered sorbitol. As a result, the invention is most easily described in terms which refer to those available sorbitol powders. To facilitate the discussion, the following definitions are provided for terms used throughout the specification and in the claims.
Sorbitol in a solid state may exist in an number of different crystalline forms, most commonly alpha and gamma forms. The alpha form actually includes both alpha and beta crystalline forms in equilibrium, but is commonly referred to in the art simply as alpha sorbitol. Generally used manufacturing processes do not produce either pure forms of alpha or
S'
S.
S S *55 55 S. S C 5* -6 gamma sorbitol. Sorbitol particles of predominantly one crystalline form may include amounts of sorbitol in other crystalline forms, as well as impurities such as mannitol. As used herein, the term "sorbitol" includes sorbitol containing such impurities within commercially acceptable limits.
Different manufacturing processes produce powdered sorbitol having different particle morphologies, most noticeably the particle shapes and densities. Thus gamma sorbitol produced in one manner will have a different morphology than gamma sorbitol produced by a different manner. It is most convenient o* to refer to these different morphologies by referring to the commercial manufacturer of the powdered sorbitol. As used herein the term "ICI morphology" refers to the flat, sharp-cornered or rod shaped particles characteristic of ICI G-100 gamma sorbitol currently produced by ICI Americas, Inc., Wilmington, Delaware (ICI was formerly known as Atlas S Chemical Industries, Inc.). Fig. 1 is a reproduction of a photograph of a microscopic enlargement (100X) of ICI G-100 powdered sorbitol particles. ICI G-100 sorbitol is reported to be at least 80% gamma sorbitol.
It is believed that the ICI morphology sorbitol is produced by the process described in U.S. Patent No.
3,973,041 to James W. DuRoss, which is hereby incorporated by reference.
The term "Pfizer morphology" refers to the more rounded, porous particles characteristic of Pfizer sorbitol currently produced by Pfizer Chemical Co., 235 E. 42nd Street, New York, New York 10017 ("Pfizer"). Fig. 2 is a reproduction of a photograph of a microscopic enlargement (100X) of Pfizer powdered sorbitol particles. The Pfizer morphology sorbitol is reported to be 60% to 80% gamma sorbitol.
-6 7 In a further attempt to define what is meant by "ICI morphology" and "Pfizer morphology", two samples of the respective sorbitol powders were viewed by placing them in an oil immersion and viewing them with a microscope. (The microscopic views in Figs. 1 and 2 are without an oil immersion.) The ICI G-100 particles appeared crystalline in nature, composed of longitudinally arranged, needle shaped crystals, resulting in mostly rod and rectangular shaped particles. The pieces looked fiberous, dense and, when finely divided, needle shaped.
The Pfizer A-60 product appeared as irregular o o• granular shapes with no evident crystal structure. No cleavage planes or smooth surfaces were observed. The exterior of the particles were irregular and roughly spherical, with fine relief suggesting an agglomeration. It appeared that air bubbles and irregular granular bodies were captured within the particles.
The lack of continuous crystalline composure was quite different than the observed nature of the G-100 product.
'Other sorbitol maniuacturers produce powdered sorbitol with different morphologies which have not been microscopically characterized. For example, Roquette Corporation, 1550 Northwestern Avenue, Gurnee, Illinois 60031,.sells powdered sorbitol with a particle morphology differing from those of ICI and Pfizer.
Powdered sorbitol is commercially available in different particle size distributions. For example, ICI gamma sorbitol is available in a coarse grind (#834) and also as fines (G-100). As used herein, a particle size distribution corresponding to G-100 means powdered sorbitol which has a particle size distribution within the following ranges, which are the ranges experimentally determined by sieving ICI's G-100 product: (All sieve sizes are U.S. National Standard) -7i 11 2 'i 8
H
Ii *000 4
C
0S 0 08 *4 4 6 *000 e
S
*5 B 0 retained on #60 sieve 1-3% retained on #100 sieve 20-35% retained on #200 sieve 55-75% pass through #200 sieve.
Likewise, a particle size distribution corresponding to A-60 means powdered sorbitol which has a particle size distribution within the following ranges, which are the ranges experimentally determined by sieving Pfizer's A-60 product: 3-15% retained on #60 sieve 35-55% retained on #100 sieve 32-46% retained on #200 sieve 0-25% pass through #200 sieve.
As defined herein, the particle size distribution of two types of powdered sorbitol differ significantly if the difference between the percentages of the particles which will pass through a #100 and a #200 sieve are each greater than 25%. The amounts of ICI G-100 and Pfizer A-60 sorbitol that will pass through a #100 sieve ure: *ICI G-100 at least 92% Pfizer A-60 not more than 62% The difference between these percentages is at least which is well above The amounts of ICI G-100 and Pfizer sorbitol that will pass through a #200 sieve are: ICI G-100 at least 55%; and Pfizer A-60 not more than The difference between these two percentages is at least 30% which is well above 25%. Thus, ICI G-100 and Pfizer A-60 differ significantly in their particle size distributions.
8
B
~4; The inherent properties of the powdered sorbitol may also be described by the properties of gums in which the sorbitol powder is used, such as Taber and Instron measurements, explained more fully hereafter.
Because the benefits of the invention stem from the use of at least two types of powdered sorbitol, the sorbitol content of the gum must be high enough to be of significance. Such high levels of sorbitol are typically used when the noncariogenic properties of the gum are important, sugarless gums. Also, the present invention has been found most S. useful when there are high levels of plasticizer present in the gum. Plasticizers include glycerine, propylene glycol and aqueous syrups such as hydrogenated starch hydrolysate solutions and sorbitol solutions. The invention is particularly useful in anhydrous formulations using high levels of glycerine.
In high moisture gums, the sorbitol particles are more likely to dissolve and recrystallize, changing their particle size-and morphology over time, and reducing the benefits provided to the gum texture by the 5 invention.
Depending on.the other gum ingredients and the types of sorbitol powder in use, the range of ratios between the types of sorbitol powders can vary from 90:10 to 10:90. When using sorbitol powders with different particle size distributions, a range of coarse to fine sorbitol powder ratios of 40:60 to 90:10 has been found most useful. In some high glycerine content gums (over a coarse:fine sorbitol ratio of 70:30 has been found most useful. ICI G-100 and Pfizer A-60 sorbitol have been found to provide a good combination of powdered sorbitols for use in practicing the various aspects of the invention.
9- 1 11 i 1 4
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10 Tests were conducted to provide some guidance as to the importance of the kinds of differences (crystalline form, morphology, and particle size) between the types of sorbitol to be used in making gum formulations. In the tests, four sample batches of gum were produced. The formulations of all gums included: 26.0% gum base so .000 0 OS 09
S
55 22.0% glycerine talc 1.1% flavor 0.6% lecithin food acids 0.4% aspartame 0.2% color The remaining 44.7% of the gum was powdered sorbitol. In each case the gum included 35.7% Pfizer powdered sorbitol and 9.0% of a different powdered sorbitol as follows: Formulation Powdered Sorbitol A ICI G-100 B Roquette "G-100" C. Pfizer "A-100" D ICI 834 The Roquette "G-100" and Pfizer "A-100" are not commercially available. For purposes of the test, Roquette "G-100" was produced by grinding and sieving Rwquette gamma sorbitol and collecting the fraction which passed through a #100 sieve. Likewise, Pfizer "A-100" was produced by grinding and sieving Pfizer sorbitol (60-80% gamma) and collecting the fraction which passed through a #100 sieve. ICI 834 is a commercially available gamma sorbitol having an ICI morphology and a particle size distribution (experimentally determined for one sample) as follows: 10 11 8% retained on #40 sieve 35.4% retained on #60 sieve 17.9% retained on #80 sieve 11.1% retained on #100 sieve 8.9% retained on #120 sieve 19.3% retained on #200 sieve pass through #200 sieve Thus, each of the four formulations contained two different types of powdered sorbitol, though one of the two types was the same in each sample. The only Sdifference between each sample was that 20% of the powdered sorbitol differed. Compared to the ICI G-100 sorbitol used in Formulation A, the control, the second type of sorbitol powder in the other formulation varied "o in the following characteristic: B morphology C crystalline form (partially) and morphology D particle size distribution.
e.°t Sensory evaluation of the three samples oe compared to the control, specifically evaluating te;Pture and flavor and sweetness release, produced the .following commentary: A vs. B: B has a firmer initial chew. In the intermediate it becomes softer and slightly slippery. It is more cohesive and squeakier in the final.
The flavor is released more slowly and there is a low impact of flavor and tartness. The i flavor character is not as round and not as balanced.
A vs. C: The texture profile of these samples is similar. C is slightly drier initially. In the final the bubbles are very slightly tougher because C is slightly firmer and more cohesive.
11 i* I VI 12 The tartness is higher in C and it is not as balanced with flavor as A (control). In the final, there is less residual flavor.
A vs. D: Initially D is firmer and drier. The final is less cohesive but it is firmer and more rubbery. It has poorer bubbles.
The flavor of D is slower releasing and the impact is lower. The flavor, tartness and sweetness are less balanced and present at lower levels throughout.
As a generalization, it was concluded that a difference in particle size distribution was the most significant contributor in the gums' final characteristics, followed by morphology and possibly crystalline form. Because of the complex nature of gum systems, and the wide variety of ingredients used, it is not possible to provide firm rules regarding the types of sorbitol-powder and the ratios which will optimize a. processability and texture characteristics of gum formulation. However, from the above results and familiarity with other formulation work, some general S. guidelines for practicing the present invention are recognizable. If the sample gum is too lumpy, dry, brittle or firm, the ratio of small particle size to t large particle size powdered sorbitol should be increased. If the sample is too soft or its rope is wavy, less fine particles should be used. Also, the use of an ICI morphology sorbitol tends to give a smoother rope, also making the gum soft, whereas Pfizer morphology sorbitol tends to produce a less sticky, dry gum with body, and a rougher rope. The Roquette gamma sorbitol appears to behave more like the Pfizer morphology sorbitol than like the ICI morphology sorbitol.
12 ;j I 5845/6 ~Cb- Igk- r 1 1 4 t 13
II
The sorbitols may also be described by properties of chewing gum in which they are used. Also, by using a standard formula and using different sorbitol powders in making the formula, the inherent property of the sorbitol may be cataloged by virtue of the measured properties of the gum. The following standard sorbitol property testing gum formula (hereinafter referred to as "the SSPT gum formula") is used for purposes of the present application: stick gum base 25.0% 4444 4 4 C 4 4 4 4 44 44 4 4O 4 t 04 sorbitol 51.2% glycerine 17.0% mannitol flavor 0.8% The above formula was prepared using two different types of sorbitol powder, ICI 834 and Pfizer A that was sieved to approximately the same particle size distribution as ICI 834. In each formulation, the base was a stick gum base with-a softening point of 670C and a cone and plate viscosity of 25,500 cps at a speed of 96.0/sec.
The SSPT gum formula was prepared by adding 500 grams of gum base to the mixer at time 0, followed by 500 grams of sorbitol. After one minute of mixing, 524 grams of additional sorbitol was added. After an elapsed mixing time of six minutes, 340 grams of 99% glycerine was added, followed by 120 grams of mannitol (ICI Mannitol 100) two minutes later. Finally, after minutes of mixing, 16 grams of "spearmint" flavor was added. Mixing was continued for five minutes, and the formulations were then sheeted and cured for 18 hours under typical commercial condition.
A Teledyne Taber machine, model 150-B, was used to measure the Taber valve of sticks of gum from each formulation. The sticks were 3/4" wide and 0.076" thick. Also, an Instron testing machine, model 1122, was used to determine the hardness. The statistical 13 14 analysis of the measurments are listed below for each formulation.
Pfizer A ICI G Taber average 58.4 33.3 number tested 5 standard deviation 1.7 2.8 Instron hardess average 74.30 63.20 number tested 25 24 standard deviation 1.22 1.93 As seen from the above, the Taber and Instron different, even though both were made from the SSPT gum formula and only the type of sorbitol powder used in each gum differed. Thus, the inherent property of the sorbitol measured by measuring the properties of the gum made from the sorbitol as used in the SSPT gum S aformula is an additional characteristic by which I4rt sorbitol powders may be differentiated for purposes of the present invention.
Generally, a confidence interval at or above indicates statistical significance. For purposes i of describing the present invention, sorbitols which produce gums having a significant statistical difference in Taber values or in Instron hardness values when made into gums of the SSPT gum formula are considered to be different types of powdered sorbitol.
As a practical matter, it is believed that using such different types of powdered sorbitol in other formulas will produce statistically significant differences in Taber and Instron hardness values.
Therefore, formulas other than the SSPT formula will probably be suitable and may be used for convenience to 14 1 1 r o d u e g m s h v i n g a s g n i f c a n t s t a i s t i a l difernce n Tber alus o in nston hrdnss determine whether sorbitol powders are different for purposes of the present invention. Further, one method of optimizing chewing gum formulations pursuant to the present invention is to produce successive batches of the gum using the same formula each time but using two or more different types of sorbitol powder, and vary only the relative ratio of the two or more types of sorbitol powder in each batch such that the Taber value or the Instron hardness value (or both) changes by a statistically significant amount between successive batches. Of course, as the optimum is approached, the o00 4 Von, Taber and Instron hardness values between successive batches will not vary by statistically significant S• amounts because the variance in the ratios of sorbitol o powders will not need to be varied as much.
c Taber values may only be measured for stick gums, but Instron tests may be conducted on both stick and chunk gums.
Because 6f the range and numbers of variations in gum compositions to which the present invenop tion may be used, representative examples of various aspects of the present invention are provided.
a The following two illustrations provide examples of practicing the invention of optimizing processability and texture by varying the ratio of the two different types of powdered sorbitol used in the gum formulations. In Example 1, a series of seven sample batches of strawberry flavored sugarless bubble gum were made. Below each batch formulation is a description of the processability and texture characteristics of the gum made. Note that Formula 1A j used only one type of sorbitol powder. It was made several months before the remaining formulas. Also, note that in Formulas 1A, 1B and 1C, three different *I flavors were used, while Formulas 1D-1G all used the i 1 5 J 1 -2- -16same flavor as Formula lB. Further, note that lB and 1E were identical formulations, as were ID and IF, but were made on different dates.
~116 p1 :a: :ir -I.-LI^YJFli U~ I 00 0 0 «0 040 0 04 00 A. 0a 0 0 a O 00 *I 00 0 000 0 000 0 0 0 4 0 0 00 o o 0 0 0, 00 0 0 00 0 0 40 4 EXAMPLE 1
FORMULA
ICI-834 Sorbitol ICI-100 Sorbit ol Pfizer Sorbitol Hydrogenated Starch Hydrolysate Solids) Base Glycerin Flavor Sorbitol Solution Solids) Talc 44.50% 0 0 6.16 24.00 8.30 0.8* 8.50 0 9.00 36.18 0 9.00 36.48 0 8.94 35.94 0 9.00 36.18 8.94 35.94 0 11.75 35.93 26.00 22.00 0.5** 0 26.00 22.00 0 26.00 22.00 0.5** 0 26.00 22.00 0.5** 0 4.00 26.00 22.00 0.5** 0 4.00 24.00 22.00 0 4.00 4.00 NOTE: Remaining is fillers, acids, and colour.
Sticky/wet Poor web Sticky/soft Poor web Good Stretch No web Moderately sticky Smooth, Extrudes even rope well Good Stretch No web Moderately sticky Breaking rope Extrusion Some stickiness on rollers Smooth, even rooe- Extrudes well Breakage Runs wraps very well rope broke a lot Inconsistent Wrapping "appears to Inconsistent; wrap" 1 batch 5 min.
longest. Another min.
longest run flavour flavour "C" Skinny rope longest run 8 minutes Longest 10 min.
Skinny rope 18 min.
Longest 27 min.
flavour KEH/0051f kIjz%~i 4 18 Example 2 shows a method of optimization including a series of six sample batches of peppermint flavored sugarless bubble gum that were made. Below each batch formulation is a description of the processability and texture characteristics of the gum made in that sample batch. Note that Formulas 2B and 2C are identical except that 2C w'as made using part of the gum made from formulation 2B to represent an amount of trim typically used in the commercial manufacture of chewing gum.
o 4 a 1 oo 'eta 18 at
I
I o 5 18 1** i 1~c w\ r; r a 9o**h a 4 a a 0o 0 a a a o Bo a a Ca CC 1
FORMULA
ICI-G100 Sorbitol Pfizer A-60 Sorbitol Base Glycerin Flavor Calcium Carbonate
NOTE:
Gum Comments: 2A 14.04% 32.76 24.00 22.10 1.00 5.00 18.72 28.08 24.00 22.10 1.00 5.00 EXAMPLE 2 2C 18.72 28.08 24.00 22.10 1.00 5.00 2D 23.40 23.40 24.00 22.00 1.00 5.00 2E 23.50 23.50 24.00 22.00 1.00 5.00 2F 28.20 18.80 24.00 22.10 1.00 5.00 Remaining is acids and color.
Firm Sticky Good stretch Firm Sticky Good stretch Tough/Dry Slightly firm Sticky Good stretch Extruder Comments: Not sticky, but some pinching Firm gum breaking in tunnel Firm, not damp, slightly sticky rough still pinching.
Needs more G-100 Very dry Very Smooth Firm, great stretch web, Slightly sticky Sticky damp gum soft sticky for wrapping. Inconsistent rope Wavy Sticky, wet, lumpy rope 3 minutes longest run bad run Very Very web, good Firm smooth good sticky stretch Not sticking to belts a little damp but firm.
High extruder RPM causing irregular rope size Wet, sticky, lumpy 10 minute run longest Very Sticky Great stretch web, Soft, Mixer a bit hot Longer mixing Wavy rope but less breaking due to higher extruder temperature 16 minute run 11 minute run Sticky, wet gum Wrapping Comments: Rough rope 1 rope breakage 1 jam in tunnel No buildup on rollers 4 minutes longest run Wavy rope Breakage Soft gum Rope breaks Weak points Extruder equipment problems Breakage Stickier buildup 13 minutes longest run KEH/0051f
C
-L
S- 6- Prior to the discovery of the present invention, one reformulation project required over 50 sample batches of gum to optimize the formulation. By using the optimization process of the present invention, it is believed that a comparable reformulation could be achieved making five sample batches or less.
The next illustration provides an example of manufacturing gum using the present invention. Example 3 depicts a production size batch of sugarless chunk bubble gum mixed and processed using standard chewing gum equipment such as is well known in the art.
a EXAMPLE 3 o' A mixer is heated to 100-140 0 preferably o° about 115 0 and maintained. With the mixer running, o"o 240 Ibs. of pelletized Ladco Bubble Base T #32781 is added and masticated for 5 to 15 minutes, preferably about 7 minutes. To this is added 220 Ibs of 99% glycerine, 1 lb. of red color dispersion and 8 lbs. of 9oo', lecithin, which are mixed for 2 to 8 minutes, ei preferably about 4 minutes. Next, 326 Ibs. of Pfizer sorbitol is added over about 2 minutes, 140 lbs.
o :7 7 of ICI G-100 sorbitol is added over about 1 1/2 minutes, and 50 Ibs. of calcium carbonate is added over about 15 seconds. The batch is mixed for 5 to o minutes, preferably about 10 minutes. Next, 0.8 lb. of o NutraSweet and 2.2 Ibs of shellac encapsulated SNutraSweet are added over about 15 seconds, and mixed for 1 to 3 minutes. The last ingredient is 12 lbs. of flavor, which is mixed 4 to 12 minutes, preferably 5 minutes, after addition.
The batch is unloaded, tempered for minutes to 2 hours at room temperature, extruded and sized to a diameter of about 0.6-0.7 inches, cooled to about 70 0 F, sized and wrapped.
product: (All sieve sizes are U.S. National Standard) 7 ~l~c
',F
i i ii .1:
HI
ai ~7pi 21 When using powdered sorbitol, it is advantageous to add the ingredients in an order least likely to result in sorbitol spots. It is believed that if powdered sorbitol is added to the mixer when the gum is stiff, the sorbitol will tend to get packed into corners of the mixer. Later, the powdered sorbitol may break free at a time when it will not get completely mixed, resulting in sorbitol spots. Since the finer sorbitol powder does the least to make the gum hard, it could be added first if spots are encountered. Also, if scrap gum is to be reworked, it should be added after the sorbitol has been mixed in, since the rework gum also tends to make the gum in the mixer stiffer.
Examples 4-8 provide examples of different chewing gum formulations which have been made in accordance with the present invention.
r4 (4 4 (4 44 P ,42 i 4 42 Base Calcium Carbonate Flavor ICI G-100 Sorbitol Pfizer A-60 Sorbitol Glycerine Mannitol Aspartame Color EXAMPLE 4 24.0% 6.0% 2.0 11.16% 33.49% 17.0% 6.0% 0.3% 0.05% EXAMPLE 5 24.0% 6.0% 2.0% 33.49% 11.24% 17.0% 6.0% 0.22% 0.05% EXAMPLE 6 24.0% 33.49% 11.16% 17.0% 0.3% 0.05% The gum of Example 4 was found to be firmer initially (with the high level of coarse Pfizer sorbitol) compared to Examples 5 and 6. The gum of Example 5 was softer initially.
21 8 ol 22 Base Calcium Carbonate Atlas 712 Sorbitol Lecithin Glycerine Mannitol Aspartame Color Flavor ICI G-100 Sorbitol EXAMPLE 7 24.0% 6.0% 44.40% 1.0% 17.0% 6.0% 0.35% 0.05% 1.2% 0:0% EXAMPLE 8 24.0% 22.32% 17.0% 0.30% 0.06% 22.32% I trr€ t t t t t 4444 I It 4 4I 4 44 t t S( 4 t 4 t( i 44 i 4 t t t The gum of Example 8 was found to chew much better than the gum of Example 7, being less gritty. The gum of Example 8 also mixed less sticky.
Examples 9 and 10 provide illustrations of the preferred embodiments of gum compositions according to the present invention. Example 9 is for a fruit flavor sugarless chunk bubble gum, and Example 10 is for a grape flavor sugarless chunk bubble gum.
I
Pfizer A-60 sorbitol ICI G-100 sorbitol Base Glycerine Calcium Carbonate Talc Flavor Lecithin Color Aspartame Food Acids EXAMPLE 9 32.6% 14.0% 24.0% 22.0% 5.0% 0.0% 1.2% 0.8% 0.1% 0.3% 0.0% EXAMPLE 35.7% 26.0% 22.0% 0.0% 1.1% 0.6% 0.2% 0.4% 22 9 23 In many instances, it is undesirable to vary the level of components such as gum base, plasticizer, moisture, bulking agents, etc. which traditionally ±iave 1I been varied to account for negative processing characteristics in a gum reformulation project. In the present invention, where two types of sorbitol powder are used, it may be possible to leave all ingredient levels the same and still optimize the texture and processability of the gum by varying only the ratio of the types of sorbitol.
In the preferred optimization process, Pfizer and ICI G-100 are used. As the level of plasticizer (glycerine for example) decreases, the ratio of Pfizer A-60 to ICI G-100 may be reduced to account for S« the change. By changing the amount and ratio of the types of sorbitol, the processing characteristics such as mixing, extrusion and sizing properties, and flexibility, stickiness and wrappability may be improved.
Also a soft gum that is not sticky, preferable to the Ct 4 majority of consumers, can be produced.
o4 As an additional benefit, sweetness release and perception of a gum formulation can also be modified by using a blend of two types of sorbitol powder in the gum. Smaller particle sizes dissolve more quickly, producing sudden sweetness. By using some larger particle sizes, a slower sweetness release is obtained. Flavor release is also affected by sweetness release, and can be improved by use of the present invention.
The processability characteristics of gum compositions of the present invention should be such that the gum can be wrapped at a rate of 800 pieces per minute or more, and be continuously fed for periods of minutes or longer. By use of the present invention, it is possible to manufacture a high glycerine content, anhydrous, sugarless, chunk gum on conventional sugar, 23 li- 1 -i 24 chunk gum equipment. In addition, in such gums the use of the two types of sorbitol can control the softness of the gum without increasing the level of gum base in the gum, which would negatively affect cost and create other problems.
The preferred embodiments of the invention relate to sugarless chunk gum. It is believed that stick gums (which are easier to process) would also benefit by use of the present invention. Stick gums are usually sheeted and scored, then allowed to stand for 24 hours or more before being wrapped. The present invention may be used to improve the gum texture and :f Ssweetness characteristics of stick gum, and also to reduce the time (and hence storage space required) between when the gum is scored and when it is wrapped.
The invention has been described with examples using two different types of sorbitol powders.
The use of three or more types of sorbitol powders is also contemplated, though it is noted that for the most I.t part, adequate advantages can be achieved using only two types of sorbitol powders.
It should be understood that a wide range of changes and modifications can be made to the preferred i embodiments of the invention described above. For example, it is recognized that in the future the characteristics (including particle morphology and particle size distribution) of commercially available sorbitol may change. The definition of "significantly different" particle size distributions, basad upon the #100 and #200 sieve sizes, might not always be easily determined. Even though the amounts of sorbitol powder that will pass through these sieve sizes are good reference points, other sieve sizes may need to be considered in determining particle size distributions which provide significant differences in texture and 24 25 processability characteristics of gum compositions. On the other hand, as specified above, the Taber and Instron hardness values of guiis made with new commercially available sorbitol powders will be useful in determining whether the powdered sorbitols differ for purposes of practicing the invention.
It is therefore intended that the foregoing detailed descriptions be regarded as illustrative rather than limiting, and that it be understood that it is the following claims, including all equivalents, which are I intended to define the scope of the present invention.
flit 4444 !4 4 4 n, 4444aiiy hrceitiso u omoiin.O
Claims (14)
1. In a process of developing a new or reformula- ted cLewing gum composition containing gum base, bulking and/or sweetening agents including powdered sorbitol, plasticizers and optional fillers, flavors, colors and processing aids, comprising the steps of 1) making a sample batch of a gum composition, 2) evaluating the texture and processability of the sample and 3) produc- ing and evaluating subsequent sample batches with dif- ferent amounts of ingredients until acceptable texture and processability characteristics are obtained, the improvement comprising: a) using at least two different sorbitol powders in one or more of the sample batches, wherein the sorbitol powders produce statistically significant differences in at least one of the values selected from the group consisting of Taber and Instron hardness when made into gums of the same formula, and b) varying the ratio between the at least two sorbitol powders in subsequent sample batches to S.improve the texture and processability characteristics 4A of the gum formulation. S2. The improved process of claim 1 wherein the at least two sorbitol powders produce a statistically significant difference in the Taber value when made into gums of the same formula.
3. The improved process of claim 1 wherein the at least two sorbitol powders produce a statistically significant difference in the Instron hardness value when made into gums of .he same formula. 26 :i j t -27-
4. The improved process of claim 1 wherein the at least two sorbitol powders comprise only two powdered sorbitols. The improved process of claim 1 wherein the sample batches of gum comprise about 15% or more of a plasticizer chosen from the group consisting of glycerine, propylene glycol, hydrogenated starch hydrolysate syrups, sorbitol solutions and mixtures thereof. 440 04, 04 Of *0 1 4, 4 440 0 4, 4 0000 00 4 Ak'
6. In a process of manufacturing chewing gum comprising the steps of 1) providing ingredients for use in the gum composition, including gum base, bulking and/or sweetening agents including powdered sorbitol, plasticizers and optional fillers, flavors, colors and processing aids, and optional fillers, flavors, colors and processing aids, 2) mixing the ingredients, and 3) processing the resulting gum composition into individual servings of gum; the improvement comprising: a) providing the powdered sorbitol in the form of at least two sorbitol powders which produce statistically significant differences in at least one of the values selected from the group consisting of Taber and Instron hardness when made into gums of the same formula.
7. The improved process of claim 6 wherein the at least two sorbitol powders produce a statistically significant difference in the Taber value when made into gums of the same formula.
8. The improves process of claim 6 wherein the at least two sorbitol powders produce a statistically significant difference in the Instron hardness value when made into gums of the same formula. 27 0( 4 r I Kr- 15 V -28-
9. The improved process of claim 6 wherein the at least two sorbitol powders comprise only two sorbitol powders. The improved process of claim 6 wherein the gum comprises about 15% or more of a plasticizer chosen from the group consisting of glycerine, propylene glycol, hydrogenated starch hydrolysate syrups, sorbitol solutions and mixtures thereof.
11. The improved process of claim 6 wherein the gum is a sugarless gum.
12. The improved process of claim 9 wherein the ratio of the two sorbitol powders is between about 90:10 and 10:90.
13. The improved process of claim 6 wherein the gum comprises bubble gum.
14. A chewing gum composition comprising gum base, plasticizer and optional fillers, flavors, colors S and processing aids, and bulking and/or sweetening agents including, when first manufactured, a first and a second sorbitol powder wherein the properties of the two sorbitol powders are such that when used to make gums of the same formulation, either the Taber or Instron hardness values of the two gums differ by a statistically significant amount. A chewing gum composition of claim 14 comprising: 14-45% gum base,
25-60% powdered sorbitol, 15-25% glycerine, -28- K 1 -16 I a- 29 wherein the powdered sorbitol comprises a ratio of 90:10 to 10:90 of said first sorbitol powder to said second sorbitol powder. 16. The composition of claim 14 wherein the chewing gum composition comprises a bubble gum composition comprising about: 24% bubble gum base,
32.6% first sorbitol powder, 14% second sorbitol powder, S22% glycerine, and S flavor and optional ingredients such as fillers, soften- Sers, color, food acids and high intensity sweeteners. o 0 0 17. The composition of claim 14 wherein the chewing gum composition comprises a grape flavored bubble gum composition comprising about: 26% bubble gum base,
35.7% first sorbitol powder, S1 9% second sorbitol powder, o 22% glycerine, and o flavor and optional ingrediets such as fillers, softeners, color, food acids and high intensity sweeteners. 18. The chewing gum composition made according to the improved process of Claim 6. 19. In a process of developing a new or reformula- ted chewing gum composition containing gum base, bulking and/or sweetening agents including powdered sorbitol, plasticizers and optional fillers, flavors, colors and processing aids, comprising the steps of 1) making a sample batch of a gum composition, 2) evaluating the texture and processability of the sample and 3) produc- ing and evaluating subsequent sample batches with dif- ferent amounts of ingredients until acceptable texture 29 plasiciers nd ptinal illrs, lavrscolos ad prcssn ais opiigtestp f1 aiga 30 and processability characteristics are obtained, the improvement comprising: a) using at least two different sorbitol powders in one or more of the sample batches, and b) varying the ratio between the at least two sorbitol powders in a subsequent sample batch such that either the Taber value or Instron hardness value differ by a statistically significant amount between the two batches. A process of developing a new or reformulated chewing gum composition, substantially as herein described with reference to Example 3. S, 21. A chewing gum composition, substantially as herein described with reference to Example 1 and any one of Formulas 1B to 1G, Example 2 and S any one of Formulas 2A to 2F or any one of Examples 3 to 6 or 8 to 22. The product of the process of any one of claims 1 to 13, 19 or S I A t J 4- DATED this TWENTY-FIRST day of MARCH 1990 Wm. Wrigley Jr. Company S I C@ 4 S I S Patent Attorneys for the Applicant SPRUSON FERGUSON 4'( I I 4 S KEH/0051f i i.
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US025939 | 1987-03-16 | ||
US07/025,939 US4803083A (en) | 1987-03-16 | 1987-03-16 | Method of optimizing texture and processability of chewing gums and compositions made therefrom |
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AU52300/90A Ceased AU622303B2 (en) | 1987-03-16 | 1990-03-27 | Method of optimizing texture and processability of chewing gums and compositions made therefrom |
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US4959226A (en) * | 1987-03-16 | 1990-09-25 | Wm. Wrigley Jr. Company | Method of optimizing texture and processability of chewing gums and compositions made therefrom |
CA2029069A1 (en) * | 1989-11-07 | 1991-05-08 | Mansukh M. Patel | Chewing gum with improved sweetness profile incorporating finely ground bulk sweetener without starch |
US5139797A (en) * | 1990-04-27 | 1992-08-18 | Leaf, Inc. | Stabilized sweetener compositions, chewing gum compositions containing same and methods for their preparation |
US5085872A (en) * | 1990-08-16 | 1992-02-04 | Wm. Wrigley Jr. Company | Method of manufacturing a chewing gum base |
WO1993005662A1 (en) * | 1991-09-17 | 1993-04-01 | Wm. Wrigley Jr. Company | Mannitol/sorbitol rolling compound blend |
US5405623A (en) * | 1993-09-22 | 1995-04-11 | Wm. Wrigley Jr. Company | Chewing gum compositions and methods for manufacturing same |
FR2715538B1 (en) * | 1994-02-01 | 1996-04-26 | Roquette Freres | Chewing gum composition having improved organoleptic quality and method for preparing such chewing gum. |
GB9403484D0 (en) * | 1994-02-24 | 1994-04-13 | Cerestar Holding Bv | Tabletting process |
US20080014302A1 (en) * | 2004-08-25 | 2008-01-17 | Cadbury Adams Usa Llc | Multi-region chewing gum composition including isomalt gum region |
MX2008010795A (en) * | 2006-02-24 | 2008-09-01 | Cadbury Adams Usa Llc | Liquid-filled chewing gum composition. |
FR3003135B1 (en) * | 2013-03-12 | 2020-10-02 | Syral Belgium Nv | PROCESS FOR IMPROVING THE ORGANOLEPTIC PROPERTIES OF SUGAR-FREE CHEWING GUM BASED ON SORBITOL |
EP3003059A1 (en) * | 2013-05-31 | 2016-04-13 | Intercontinental Great Brands LLC | Chewing gum with hard, amorphous inclusions; and methods of making thereof |
BE1021954B1 (en) * | 2014-06-05 | 2016-01-28 | Syral Belgium Nv | COMPOSITION OF SORBITOL WITH LOW FRIABILITY |
WO2016140995A1 (en) * | 2015-03-05 | 2016-09-09 | Intercontinental Great Brands Llc | Process of using sorbitol of small and large crystal sizes to achieve gum texture and chewing gum including the sorbitol combination |
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US4217368A (en) * | 1977-07-08 | 1980-08-12 | Life Savers, Inc. | Long-lasting chewing gum and method |
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US2315699A (en) * | 1939-07-27 | 1943-04-06 | Atlas Powder Co | Crystallization of sorbitol |
US2483254A (en) * | 1946-01-03 | 1949-09-27 | Atlas Powder Co | Production of dry sorbitol |
US2594863A (en) * | 1948-12-24 | 1952-04-29 | Atlas Powder Co | Crystallization of sorbitol |
US3330874A (en) * | 1963-01-31 | 1967-07-11 | Pfizer & Co C | Sorbitol crystallization process |
US3308171A (en) * | 1964-07-17 | 1967-03-07 | Yokohama Seito Kabushiki Kaish | Method for producing granular or powdery sorbitol from sorbitol solution |
US3973041A (en) * | 1976-03-03 | 1976-08-03 | Ici United States Inc. | Sugarless chewing gum having improved shelf life |
US4293570A (en) * | 1979-04-02 | 1981-10-06 | Chimicasa Gmbh | Process for the preparation of sweetener containing product |
US4316915A (en) * | 1979-10-01 | 1982-02-23 | Life Savers, Inc. | Center-filled chewing gums |
US4252794A (en) * | 1979-12-20 | 1981-02-24 | Ici Americas Inc. | Gamma-sorbitol polymorph |
US4388328A (en) * | 1981-10-15 | 1983-06-14 | Warner-Lambert Company | Sorbitol containing mixture encapsulated flavor |
US4448789A (en) * | 1982-08-27 | 1984-05-15 | Warner-Lambert Company | Enhanced flavor-releasing agent |
DE3245170A1 (en) * | 1982-12-07 | 1984-06-07 | Merck Patent Gmbh, 6100 Darmstadt | IMPROVED SORBITE, METHOD FOR THE PRODUCTION AND USE |
US4545392A (en) * | 1983-07-25 | 1985-10-08 | R. J. Reynolds Tobacco Co. | Tobacco product |
US4536396A (en) * | 1983-09-06 | 1985-08-20 | Pfizer Inc. | Synergistic sweetening compositions |
CA1240875A (en) * | 1984-01-31 | 1988-08-23 | Subraman R. Cherukuri | Tableted chewing gum composition and method of preparation |
US4588592A (en) * | 1984-07-18 | 1986-05-13 | Fleer Corporation | Chewing gum product and composition and process for the preparation thereof |
FR2575038B1 (en) * | 1984-12-21 | 1990-03-16 | Roquette Freres | SUGAR-FREE CHEWING GUM AND MANUFACTURING METHOD THEREOF |
US4582707A (en) * | 1984-12-26 | 1986-04-15 | Nabisco Brands, Inc. | Non-sticking chewing gum |
US4806364A (en) * | 1987-04-22 | 1989-02-21 | Wm. Wrigley Jr. Company | Method of making chewing gum |
US4780324A (en) * | 1987-06-23 | 1988-10-25 | Warner-Lambert Company | Chewing gum with long lasting softness |
-
1987
- 1987-03-16 US US07/025,939 patent/US4803083A/en not_active Expired - Lifetime
-
1988
- 1988-03-09 NZ NZ223820A patent/NZ223820A/en unknown
- 1988-03-14 JP JP63503155A patent/JPH01503118A/en active Pending
- 1988-03-14 AU AU15998/88A patent/AU594618B2/en not_active Ceased
- 1988-03-14 EP EP88903513A patent/EP0304483B1/en not_active Expired - Lifetime
- 1988-03-14 DE DE88903513T patent/DE3885042T2/en not_active Expired - Fee Related
- 1988-03-14 PH PH36634A patent/PH25162A/en unknown
- 1988-03-14 WO PCT/US1988/000697 patent/WO1988006845A1/en active IP Right Grant
- 1988-03-15 ES ES8800768A patent/ES2006110A6/en not_active Expired
- 1988-03-15 CA CA000561441A patent/CA1333022C/en not_active Expired - Fee Related
- 1988-11-15 DK DK198806383A patent/DK174930B1/en not_active IP Right Cessation
- 1988-11-15 KR KR1019880701477A patent/KR890700315A/en not_active Application Discontinuation
- 1988-11-15 FI FI885274A patent/FI93077C/en not_active IP Right Cessation
-
1990
- 1990-03-27 AU AU52300/90A patent/AU622303B2/en not_active Ceased
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US4217368A (en) * | 1977-07-08 | 1980-08-12 | Life Savers, Inc. | Long-lasting chewing gum and method |
US4208431A (en) * | 1978-05-05 | 1980-06-17 | Life Savers, Inc. | Long-lasting chewing gum having good processibility and method |
Also Published As
Publication number | Publication date |
---|---|
DE3885042D1 (en) | 1993-11-25 |
AU594618B2 (en) | 1990-03-08 |
EP0304483A1 (en) | 1989-03-01 |
FI93077B (en) | 1994-11-15 |
DE3885042T2 (en) | 1994-02-10 |
DK638388A (en) | 1988-11-15 |
PH25162A (en) | 1991-03-27 |
US4803083A (en) | 1989-02-07 |
AU1599888A (en) | 1988-10-10 |
EP0304483A4 (en) | 1989-04-12 |
FI885274A (en) | 1988-11-15 |
KR890700315A (en) | 1989-04-24 |
AU5230090A (en) | 1990-08-02 |
ES2006110A6 (en) | 1989-04-01 |
EP0304483B1 (en) | 1993-10-20 |
DK174930B1 (en) | 2004-03-01 |
FI93077C (en) | 1995-02-27 |
NZ223820A (en) | 1991-07-26 |
WO1988006845A1 (en) | 1988-09-22 |
FI885274A0 (en) | 1988-11-15 |
CA1333022C (en) | 1994-11-15 |
DK638388D0 (en) | 1988-11-15 |
JPH01503118A (en) | 1989-10-26 |
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